Single base-pair substitutions at the translation initiation sites of human genes as a cause of inherited disease. (Record no. 20936457)

MARC details
000 -LEADER
fixed length control field 01320 a2200397 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250516042901.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 201201s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1098-1004
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1002/humu.21547
Source of number or code doi
040 ## - CATALOGING SOURCE
Original cataloging agency NLM
Language of cataloging eng
Transcribing agency NLM
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Wolf, Andreas
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20120117
245 00 - TITLE STATEMENT
Title Single base-pair substitutions at the translation initiation sites of human genes as a cause of inherited disease.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Human mutation
Date of publication, distribution, etc. Oct 2011
300 ## - PHYSICAL DESCRIPTION
Extent 1137-43 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Journal Article
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element 5' Flanking Region
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Codon, Initiator
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Consensus Sequence
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Databases, Genetic
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Genetic Diseases, Inborn
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Humans
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Mutation Rate
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Open Reading Frames
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Peptide Chain Initiation, Translational
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Point Mutation
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Caliebe, Amke
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Thomas, Nick S T
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Ball, Edward V
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Mort, Matthew
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Stenson, Peter D
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Krawczak, Michael
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Cooper, David N
773 0# - HOST ITEM ENTRY
Title Human mutation
Related parts vol. 32
-- no. 10
-- p. 1137-43
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1002/humu.21547">https://doi.org/10.1002/humu.21547</a>
Public note Available from publisher's website

No items available.